IP Library Granted Patent US 8,574,584
Granted Patent B2
US 8,574,584 · App. 13/355,343 · Granted Nov 5, 2013

EphA2 T cell epitopes and uses therefor

Inventors: Walter J. Storkus (Glenshaw, PA); Michael S. Klnch (Laytonsville, MD)
Assignee: University of Pittsburgh —of the Commonwealth System of Higher Education
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Quick Facts
Patent No.
US 8,574,584
App. No.
13/355,343
Granted
Nov 5, 2013
Kind
B2
Abstract

EphA2 T-cell epitope are provided herein. The epitopes include peptides corresponding to specific fragments of human EphA2 protein containing one or more T-cell epitopes, and conservative derivatives thereof. The EphA2 T-cell epitopes are useful in an assay, such as an ELISPOT assay, that may be used to determine and/or quantify a patient's immune responsiveness to EphA2. The epitopes also are useful in methods of modulating a patient's immune reactivity to EphA2, which has substantial utility as a treatment for cancers that overexpress EphA2, such as renal cell carcinoma (RCC). The EphA2 epitopes also can be used to vaccinate a patient against EphA2, by in vivo or ex vivo methods.

Claims (10)

1. An isolated peptide that consists of 9-35 amino acid residues and wherein said isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891), where said TLADFDPRV (SEQ ID NO:2, residues 883-891) peptide (i) has up to one conservative amino acid substitution within the conservative substitution groups (a) S and T, (b) L, I and V, and (c) E and D; and (ii) retains the ability to stimulate a T-cell immune response to EphA2 as determined by ELISPOT assay.

2. The isolated peptide of claim 1 that comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891).

3. A vaccine formulation comprising an isolated peptide that consists of 9-35 amino acid residues and wherein said isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891), where said TLADFDPRV (SEQ ID NO:2, residues 883-891) peptide (i) has up to one conservative amino acid substitution within the conservative substitution groups (a) S and T, (b) L, I and V, and (c) E and D; and (ii) retains the ability to stimulate a T-cell immune response to EphA2 as determined by ELISPOT assay, and a pharmaceutically acceptable carrier.

4. The vaccine formulation of claim 3 where the isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891).

5. The vaccine formulation of claim 3 that further comprises an adjuvant.

6. The vaccine formulation of claim 4 that further comprises an adjuvant.

7. The vaccine formulation of claim 3 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

8. The vaccine formulation of claim 4 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

9. The vaccine formulation of claim 5 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

10. The vaccine formulation of claim 6 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

Assignments (1)
CONFIRMATORY LICENSE Recorded Feb 8, 2012
From: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027669/0034 →
Continuity (5)
Division 11977179 · Oct 22, 2007
Continuation 11233796 · Sep 23, 2005
Continuation 10897711 · Jul 22, 2004
Provisional Application 60491046 · Jul 30, 2003
Related Publication 20120201840A1 · Aug 9, 2012